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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1977 2
1978 2
1980 1
1981 1
1982 1
1983 5
1984 2
1985 2
1986 1
1987 4
1988 4
1989 2
1990 5
1991 6
1992 7
1993 9
1994 5
1995 7
1996 6
1997 8
1998 9
1999 15
2000 11
2001 14
2002 11
2003 6
2004 13
2005 11
2006 12
2007 15
2008 16
2009 17
2010 16
2011 18
2012 24
2013 21
2014 17
2015 17
2016 15
2017 13
2018 18
2019 10
2020 28
2021 26
2022 13
2023 15
2024 9

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Search Results

440 results

Results by year

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Page 1
Longitudinal extensive transverse myelitis--it's not all neuromyelitis optica.
Trebst C, Raab P, Voss EV, Rommer P, Abu-Mugheisib M, Zettl UK, Stangel M. Trebst C, et al. Nat Rev Neurol. 2011 Nov 1;7(12):688-98. doi: 10.1038/nrneurol.2011.176. Nat Rev Neurol. 2011. PMID: 22045269 Review.
The clinical presentation of a patient with LETM is often dramatic and can consist of paraparesis or tetraparesis, sensory disturbances, and gait, bladder, bowel and/or sexual dysfunction. ...
The clinical presentation of a patient with LETM is often dramatic and can consist of paraparesis or tetraparesis, sensory disturbanc …
Oncolytic DNX-2401 Virus for Pediatric Diffuse Intrinsic Pontine Glioma.
Gállego Pérez-Larraya J, Garcia-Moure M, Labiano S, Patiño-García A, Dobbs J, Gonzalez-Huarriz M, Zalacain M, Marrodan L, Martinez-Velez N, Puigdelloses M, Laspidea V, Astigarraga I, Lopez-Ibor B, Cruz O, Oscoz Lizarbe M, Hervas-Stubbs S, Alkorta-Aranburu G, Tamayo I, Tavira B, Hernandez-Alcoceba R, Jones C, Dharmadhikari G, Ruiz-Moreno C, Stunnenberg H, Hulleman E, van der Lugt J, Idoate MÁ, Diez-Valle R, Esparragosa Vázquez I, Villalba M, de Andrea C, Núñez-Córdoba JM, Ewald B, Robbins J, Fueyo J, Gomez-Manzano C, Lang FF, Tejada S, Alonso MM. Gállego Pérez-Larraya J, et al. N Engl J Med. 2022 Jun 30;386(26):2471-2481. doi: 10.1056/NEJMoa2202028. N Engl J Med. 2022. PMID: 35767439 Clinical Trial.
Adverse events among the patients included headache, nausea, vomiting, and fatigue. Hemiparesis and tetraparesis developed in 1 patient each. Over a median follow-up of 17.8 months (range, 5.9 to 33.5), a reduction in tumor size, as assessed on magnetic resonance imaging, …
Adverse events among the patients included headache, nausea, vomiting, and fatigue. Hemiparesis and tetraparesis developed in 1 patie …
Acute non-traumatic tetraparesis - Differential diagnosis.
Oliveira R, Ramalho Rocha F, Teodoro T, Oliveira Santos M. Oliveira R, et al. J Clin Neurosci. 2021 May;87:116-124. doi: 10.1016/j.jocn.2021.02.024. Epub 2021 Mar 20. J Clin Neurosci. 2021. PMID: 33863518 Review.
INTRODUCTION: Potentially life-threatening disorders may present in the emergency department with acute tetraparesis, and their recognition is crucial for an appropriate management and timely treatment. Our review aims to systematize the differential diagnosis of acute non …
INTRODUCTION: Potentially life-threatening disorders may present in the emergency department with acute tetraparesis, and their recog …
Axonal dystrophies.
Nardocci N, Zorzi G. Nardocci N, et al. Handb Clin Neurol. 2013;113:1919-24. doi: 10.1016/B978-0-444-59565-2.00062-9. Handb Clin Neurol. 2013. PMID: 23622415 Review.
In classic INAD patients present with psychomotor regression between 6 months-3 years, followed by neurological deterioration leading to tetraparesis, optic atrophy, and dementia. Atypical NAD refers to all patients who differ from the classical phenotype in term of age at …
In classic INAD patients present with psychomotor regression between 6 months-3 years, followed by neurological deterioration leading to …
Dengue encephalopathy.
Hendarto SK, Hadinegoro SR. Hendarto SK, et al. Acta Paediatr Jpn. 1992 Jun;34(3):350-7. doi: 10.1111/j.1442-200x.1992.tb00971.x. Acta Paediatr Jpn. 1992. PMID: 1509881
Laboratory examination showed an unusually high increase of serum transaminases, hyponatremia, and hypoxia. Neurologic abnormalities detected were hemiparesis and tetraparesis of the extremities, and second nerve atrophy; such abnormalities were found in 10 out of the 152 …
Laboratory examination showed an unusually high increase of serum transaminases, hyponatremia, and hypoxia. Neurologic abnormalities detecte …
Nicotine-sensitive paresis.
Yokota T, Kagamihara Y, Hayashi H, Tsukagoshi H, Tanabe H. Yokota T, et al. Neurology. 1992 Feb;42(2):382-8. doi: 10.1212/wnl.42.2.382. Neurology. 1992. PMID: 1736170
Immediately after a patient with myoclonus epilepsy smoked a nicotine-containing cigarette, tetraparesis and hyperreflexia with ankle clonus developed, but disappeared within several minutes. ...A similar effect occurred when the patient chewed nicotine gum, and smoking a …
Immediately after a patient with myoclonus epilepsy smoked a nicotine-containing cigarette, tetraparesis and hyperreflexia with ankle …
Atelencephaly.
Iivanainen M, Haltia M, Lydecken K. Iivanainen M, et al. Dev Med Child Neurol. 1977 Oct;19(5):663-8. doi: 10.1111/j.1469-8749.1977.tb08000.x. Dev Med Child Neurol. 1977. PMID: 913906
The patient had marmorated skin, hypoplastic penis and undescended testes. Spastic tetraparesis was present. Moro, grasp and sucking reflexes were easily elicited. ...
The patient had marmorated skin, hypoplastic penis and undescended testes. Spastic tetraparesis was present. Moro, grasp and sucking …
Repetitive Sleep Starts in Allan-Herndon-Dudley Syndrome.
Solazzi R, Nanni G, Esposito S, Estienne M, Freri E, Zibordi F, Canafoglia L, Castellotti B, Granata T. Solazzi R, et al. Pediatr Neurol. 2023 Oct;147:24-27. doi: 10.1016/j.pediatrneurol.2023.06.012. Epub 2023 Jun 22. Pediatr Neurol. 2023. PMID: 37542971
Central hypothyroidism and chronic peripheral thyrotoxicosis result in a severe phenotype, mainly characterized by poor growth, intellectual disability, spastic tetraparesis, and movement disorders, including paroxysmal ones (startle reaction and paroxysmal dyskinesias). . …
Central hypothyroidism and chronic peripheral thyrotoxicosis result in a severe phenotype, mainly characterized by poor growth, intellectual …
Diagnosis and management of Marchiafava-Bignami disease: a review of CT/MRI confirmed cases.
Hillbom M, Saloheimo P, Fujioka S, Wszolek ZK, Juvela S, Leone MA. Hillbom M, et al. J Neurol Neurosurg Psychiatry. 2014 Feb;85(2):168-73. doi: 10.1136/jnnp-2013-305979. Epub 2013 Aug 26. J Neurol Neurosurg Psychiatry. 2014. PMID: 23978380 Free PMC article. Review.
RESULTS: The mimicking conditions were differentiated from MBD by the occurrence of solitary and rapidly disappearing splenial lesions; fewer signs and symptoms with exception of seizures, hemiparesis and tetraparesis; nystagmus; and rapid and complete recovery. MBD occurr …
RESULTS: The mimicking conditions were differentiated from MBD by the occurrence of solitary and rapidly disappearing splenial lesions; fewe …
The infantile neuroaxonal dystrophy rating scale (INAD-RS).
Atwal PS, Midei M, Adams D, Fay A, Heerinckx F, Milner P. Atwal PS, et al. Orphanet J Rare Dis. 2020 Jul 29;15(1):195. doi: 10.1186/s13023-020-01479-5. Orphanet J Rare Dis. 2020. PMID: 32727524 Free PMC article.
The clinical presentation occurs between 6 months and 3 years with global developmental regression, hypotonia, and progressive spastic tetraparesis. Progression is often rapid, resulting in severe spasticity, visual impairment, and cognitive decline, with many children not …
The clinical presentation occurs between 6 months and 3 years with global developmental regression, hypotonia, and progressive spastic te …
440 results